A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556342



Internal ID16343751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107369364..107372262hg38UCSC Ensembl
Innerchr11:107240090..107242988hg19UCSC Ensembl
Innerchr11:106745300..106748198hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382899
hg192899
hg182899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2169n54
Supporting Variantsnssv784161, nssv784162
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556342
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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